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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking TYR and oculocutaneous albinism in Homo sapiens.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Blaszczyk WM, etal., Pigment Cell Res. 2005 Apr;18(2):144-5.
  • The annotation has been inferred from sequence orthology with Tyr (Rattus norvegicus) [(IAGP) inferred by association of genotype and phenotype]
  • 4 additional annotations were made from Blaszczyk WM, etal., Pigment Cell Res. 2005 Apr;18(2):144-5.
  • 107 RGD objects have been annotated to oculocutaneous albinism  (DOID:0050632)
  • 30 papers in RGD have been used to annotate TYR
  • Curation Notes: DNA:missense mutation:exon:p.R299H (rat)


    • An association has been curated linking Tyr and oculocutaneous albinism in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from Blaszczyk WM, etal., Pigment Cell Res. 2005 Apr;18(2):144-5.
  • The annotation has been inferred from sequence orthology with Tyr (Rattus norvegicus) [(IAGP) inferred by association of genotype and phenotype]
  • 4 additional annotations were made from Blaszczyk WM, etal., Pigment Cell Res. 2005 Apr;18(2):144-5.
  • 107 RGD objects have been annotated to oculocutaneous albinism  (DOID:0050632)
  • 32 papers in RGD have been used to annotate Tyr
  • Curation Notes: DNA:missense mutation:exon:p.R299H (rat)


    • An association has been curated linking Tyr and oculocutaneous albinism in Rattus norvegicus.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from Blaszczyk WM, etal., Pigment Cell Res. 2005 Apr;18(2):144-5.
  • 4 additional annotations were made from Blaszczyk WM, etal., Pigment Cell Res. 2005 Apr;18(2):144-5.
  • 107 RGD objects have been annotated to oculocutaneous albinism  (DOID:0050632)
  • 34 papers in RGD have been used to annotate Tyr
  • Curation Notes: DNA:missense mutation:exon:p.R299H (rat)


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